|
PropeciaDrug - Propecia The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Finasteride
Strength -
1MG
Applicant -
MERCK
New Drug Application (NDA) Number -
020788
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Dec 19, 1997
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Merck Research Laboratories Div Merck Co Inc
Propecia
Fexofenadine Hcl 180mg Tablet; Oral
Fexofenadine Hcl 30mg Tablet; Oral Fexofenadine Hcl 60mg Tablet; Oral Allegra D 24 Hour 180mg;240mg Tablet, Extended Release; Oral Allegra-d 12 Hour 60mg;120mg Tablet, Extended Release; Oral Fexofenadine Hcl And Pseudoephedrine Hcl 60mg;120mg Tablet, Extended Release; Oral Ibrin 154uci/vial Injectable; Injection Radionuclide-labeled (125 I) Fibrinogen (human) Sensor 140uci/ml Injectable; Injection Propecia 1mg Tablet; Oral Fexofenadine Hcl 60mg Tablet; Oral NewDrugInformation |